I am Jimena Sofia, I am 3 years old, I know what many know me, they have been with us in difficult times since my premature birth in 2017 at 27. 6 weeks gestation, clinging to life even though my life prognosis was 2% weighing barely 1060 grams, after 40 days in the NICU they were able to take me home with my parents, they were kangaroo parents, and it was the best experience, we experienced the deepest connection that can exist.
A few days after birth, I was diagnosed with a congenital defect, Lipomyelomeningocele with the anchored spinal cord, which by my condition, low weight, and extreme prematurity could not be surgically intervened at the time I was born and the medical criteria was to keep me under observation as I was growing.
Time has passed, and I already have consequences for having the spinal cord anchored, a surgical procedure of spinal cord anchorage is the only alternative we have so that I can continue to develop health and avoid more health problems in the future as I grow.
Pitifully my dad passed away last year, he fought to give me the best and looked for options abroad for my future intervention, that was his greatest wish since in our country we do not have the technological means of transoperative neuromonitoring to avoid the least possible damage.
That is why my mom and I, appeal to your big heart. We need your support for my prompt surgery in Mexico, your accompaniment in prayer is the most important thing, if you wish to collaborate economically with us, you can do it here.
Any amount you decide is well-received and appreciated.
You would make me very happy if you use the button [Collaborate sharing] to share my project!
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3 months ago
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